Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S435/00—Chemistry: molecular biology and microbiology
  • Y10S435/8215—Microorganisms
  • Y10S435/948—Microorganisms using viruses or cell lines

Definitions

• the spectrum of the human immune response may be more restricted and therefore useful for the production of monoclonal antibodies to cell surface markers, such as HLA specificities.
• the isolation of autoimmune monoclonal antibodies and their use as antigens could lead to human monoclonal anti-idiotypic therapy to regulate the responses to autoantigens or transplanted tissue antigens.
• humoral responses to infectious disease agents could be exploited to develop useful diagnostic monoclonal antibodies.
• EBV containing supernatants have previously been utilized to transform human B cells into cell lines producing polyclonal or monoclonal antibodies against NNP hapten (Steinitz et al., Nature (1979) 267:52), TPN hapten (Kozbor et al., J. Immunol. (1977) 10:181), Rh antigen (Koskimies, J. Immunol. (1979) 10:371, Boylston et al., ibid (1980) 12:255) Streptococcus A carbohydrate (Steinitz et al., Immunobiology (1979) 156:41) Tetanus toxoid (Zurawski et al., .
• B-lymphocytes capable of producing monoclonal antibodies, particularly IgG.
• An Epstein-Barr virus (EBV) transformed mammalian cell (“transferring cell”) is combined with B-lymphocytes ("recipient cells") which have been exposed to an immunogen of interest.
• the conditions of the combining result in the selective isolation of the immortalized recipient cells.
• the EBV transferring cells transfer EBV to the B-lymphocytes resulting in the immortalization of the B-lymphocytes.
• the clones are screened for production of antibodies to the desired determinant site.
• the method employs an Epstein-Barr virus ("EBV") transformed cell (normally a lymphocyte) as a transferring agent. This cell will be referred to hereafter as the "transferring cell.”
• EBV Epstein-Barr virus
• the transferring cell is combined or cocultivated under non-fusing conditions with cells capable of producing immunoglobulin (normally B-lymphocytes).
• the cells capable of immunoglobulin (“Ig”) production are transformed by cocultivation with the transferring cell, becoming immortalized and committed to Ig production.
• the cells capable of being transformed by cocultivation and committed to immunoglobulin production will be referred to as "recipient cells.”
• the transferring and recipient cells are cocultivated under selective conditions, whereby transformed recipient cells, which are now immortalized (“immortalized Ig producing cells”), can proliferate free of the transferring cells.
• immortalized Ig producing cells may be screened for the selection of those cells producing immunoglobulin against the desired ligand specificity and subsequently cloned to establish cell lines stably producing monoclonal Ig of the desired class and isotype.
• the subject method may be used for producing monoclonal antibodies of any of the immunoglobulin classes such as IgA, IgD, IgE, IgG and IgM, including the various isotypes of heavy chains e.g. IgG 1-4 .
• the monoclonal antibodies may be modified in a variety of ways, such as enzymatic and/or acid digestion, to produce specific fragments such as Fab, F(ab') 2 , F v' F d , F c' K and A light chains.
• the transferring cell may be any cell which is a host for EBV and can be selected for so as to be selectively removed after transformation and immortalization of the recipient cells.
• the cocultivation of the transferring and recipient cells is carried out under selective cytotoxic conditions for the transferring cells.
• the EBV transferring cell line to be considered are whether: It is available and can be mutated to be sensitive to a cytotoxic agent to which the recipient cells are not sensitive; it is a host for EBV and is capable of acting as a transferring cell, which upon introduction into a medium with the recipient cells, will act to transform and immortalize the recipient cells.
• EBV eBV-derived mammal cells
• Various cell lines are available which contain EBV, such as human lymphoblastoid GM 4672, marmoset line B95-8, etc.
• Various techniques may be employed for selectively separating the immortalized Ig producing cells to the virtual complete absence of the transferring cells. The techniques will depend to some degree on the differences between the transferring cells and the recipient cells. In some instances the cells may be separated or distinguished by their buoyant density. Various media e.g. Percoll, may be employed for providing regions of different density during centrifugation. Where the two groups of cells can be distinguished by surface antigens, antibodies, selective for the transferring cells, in conjunction with complement or lysing toxins may be useful.
• selective cytotoxic agents have found use.
• the selective cytotoxic agents are used where the transferring cell is sensitive to or can be sensitized to a cytotoxic agent to which the recipient cells are resistant.
• the sensitization can usually be achieved by subjecting the transferring cells to a mutagenic agent and then selecting for cells which are sensitive to a selective cytotoxic agent.
• HGPRT hypoxanthine- guanine phosphoribosyltransferase
• HAT hypoxanthine aminopterin, thymidine
• Various mutation inducing agents can be employed to facilitate the derivation of HGPRT cells, which are then sensitive to HAT.
• ethyl methanesulfonate or N-nitroso guanidine is employed; see, for example, Nature (1975) 156:495-497.
• the recipient cells may come from a wide variety of sources and hosts, with the limitation that the host must be capable of becoming an immortalized Ig producing cell. This will mean that the cell will normally be within the host range of EBV.
• B-lymphocytes may come from peripheral blood, tonsils, Peyer's patches, spleen and lymph nodes. The particular choice will vary depending on the purpose of the transformation. Usually the choice will depend upon the availablility of B-lymphocytes which are capable of producing a desired immunoglobulin to a determinant of interest. In other situations transforming a particular set of B-lymphocytes will be the goal.
• the recipient cell may be immunized in vivo or in vitro by any desirable immunogen, either haptenic or antigenic.
• the determinant site of interest may be present in a simple monomeric organic compound, either naturally occuring or synthetic, polypeptides and proteins, polysaccharide, nucleic acid, or the like, or combinations thereof.
• the compounds may function as drugs, contaminants, pesticides, pollutants, cellular members, e.g., surface membrane proteins, cytosol proteins, nucleolus proteins, etc., enzymes, hormones, antibiotics, etc.
• Whole organisms or cells may be employed, such as viruses, bacteria, fungi, protozoa, mammalian cells, etc. or parts thereof, e.g. nuclei.
• the B-lymphocytes may be activated by an immunogen in vivo or in vitro when producing an antibody to a ligand of interest.
• Hosts having undergone tonsillectomies or splenectomies can serve as sources for the particular organs.
• the host sources for the B-lymphocytes will be the primates, as indicated previously.
• the host will have been immunized at least once and frequently about two weeks prior to the removal of the organ.
• the viable mononuclear cells are suspended in an appropriate nutrient medium and non-adherent cells separated from adherent cells.
• a source of recipient cells e.g. peripheral blood lymphocytes (PBL) may be isolated and seeded in macrophage containing nutrient medium with the appropriate antigen at a sufficient concentration to provide activation. After sufficient time for priming, generally from about 2 to 4 days, the viable cells may be separated from the dead cells and employed as recipient cells.
• PBL peripheral blood lymphocytes
• the transformation of the recipient cells will normally be carried out in the substantial absence of functioning viable T-cells.
• the removal of T-cell interference to the transformation can be achieved by either substantial removal of the T-cells or by inactivation of the T-cell.
• T-cells may be accomplished by any conventional means which maintains the viability of the B-lymphocyte recipient cells.
• the T-cells may be removed by formation of E-rosettes, with sheep red blood cells, which E-rosettes may then be separated from the medium.
• the T-cells may be inactivated, for example, by employing cyclosporin A or other T-cell inactivating agent.
• the B-lymphocyte suspension which is employed should be depleted of functioning viable Tcells.
• the recipient cells depleted of active T-cells and provided as a suspension in an appropriate nutrient medium may then be cocultivated with the transferring cells for transformation of the recipient cell population.
• the two types of cells are combined in an appropriate medium, e.g. RPMI 1640, in the substantial absence of a fusogen, generally at ratios of about 0.2-5:1 of recipient to transferring cells, usually 1-3:1.
• the two cell populations are cocultivated.
• the cells may be brought into more intimate contact by any convenient means, such as centrifugation sufficient to bring the cells into close contact without damaging the cells. Centrifugation at from about 100-200 xg at room temperature for from about 1-60 minutes is normally satisfactory, preferably at least about 5 minutes.
• the cells are cocultivated and the immortalized Ig producing cells obtained free of the transferring cells by mechanical or chemical means.
• chemical means will be used which are selectively cytotoxic.
• the concentrations of the individual components will range from about 10 -4 to 10 M.
• the cell concentrations for each of the transferring and recipient cells will range from about 10 4 to 10 5 cells/ml.
• the temperature will generally be in the range of about 15°-40°C.
• the antibodies based on binding sites will be in substantial excess of the number of cells with at least sufficient amount of complement.
• the toxin e.g. diphtheria toxin or ricin toxin, will be joined to the antibody free of the non-specific binding portion of the toxin i.e. the B peptide.
• the cell suspension is plated into microtiter wells.
• the cells are incubated under growth conditions e.g. 37°C, 6% C0 2 atmosphere, and maintained under selective conditions.
• HGPRT transferring cells HAT is maintained in the nutrient medium.
• the immortalized Ig producing cells are found to emerge and proliferate in 7 to 14 days.
• the supernatants of the cells in individual wells are screened and cells in positive wells cloned under limiting dilution conditions.
• the supernatant fluid of each culture microwell can be tested for immunoglobulin production by, for example, using Staphylococcus protein A in an appropriate immunoassay e.g. 125 solid phase radioimmunoassay.
• an appropriate immunoassay e.g. 125 solid phase radioimmunoassay.
• This technique is only diagnostic of some immunoglobulins, so that detection of other immunoglobulins may be achieved by using antibodies for Fc for the particular immunoglobulin.
• Cultures producing the desired immunoglobulins are cloned in an appropriate nutrient medium.
• the growth of the clones may be in various media, such as nutrient media, nutrient media in combination with conditioned media, feeder layers or the like.
• Feeder layers include human foreskin fibroblast feeder cells, irradiated human fetal fibroblasts, lymphocyte preparations, autologous or allogeneic human PBL, mouse lymphoid cells, or the like.
• the immortalizeti-Ig producing cells may be grown in culture flasks in an appropriate nutrient medium with conventional supplements and the antibodies harvested from the supernatant or the cells injected into the peritoneum of a host which will not reject the implant, e.g., an appropriate primate or immune system deficient host, e.g. nude mouse, and the ascites collected or the immunoglobulins in the blood harvested. Any conventional technique which provides for efficient growth of the cells and production of the immunoglobulin may be employed.
• the antibodies produced by the host will be of interest, particularly a host having a disease, such as cancer, e.g. leukemia and lymphoma, an autoimmune disease, an infectious disease, and the like.
• a disease such as cancer, e.g. leukemia and lymphoma, an autoimmune disease, an infectious disease, and the like.
• the patient's blood or serum could be screened while the disease is manifested, during convalescence or after recovery.
• a source of B-lymphocytes may be taken from the host and the cells transformed in accordance with this invention to produce immortalized Ig producing cells.
• the Igs produced by the cells may then be screened using the appropriate antigen. In some instances it may be desirable to transform memory cells.
• the immortalized Ig producing cells can be used for a number of purposes other than the direct production of antibodies to the desired determinant site. Since the cells are specific for the determinant site, they will produce large amounts of mRNA coding for the chains of the immunoglobulin.
• the mRNA from the cells may be isolated free of other RNA using an oligo-dT column. The presence of the desired mRNA may be established in conventional ways with oocytes.
• the mRNA can be used as a template for ss cDNA, which with primer and DNA polymerase will provide ds cDNA.
• the mixture of ds cDNA is amplified by cloning in an appropriate vector and the amplified ds cDNA screened for the presence of a sequence coding for the Fc portion of either the heavy or light chain, using a RNA or DNA probe and hybridizing under stringent conditions, according to the Southern method.
• the ds cDNA coding for the desired Ig chain may be excised and modified by restriction using an appropriate endonuclease, primer repair or in vitro mutagenesis to provide a ds cDNA fragment which can be inserted into an expression vector and produce the desired amino acid sequence in a unicellular host.
• the light and heavy chains may be combined under renaturing conditions to produce an Ig with or without glycosidyl substituents.
• the immortalized Ig producing cells may also be used as a source of the chromosome having the genes encoding the immunoglobulin.
• the cell may be fused with a myeloma cell to produce hybridomas capable of producing the desired immunoglobulins.
• the fusogen would be a xenogenic cell which would then produce the desired antibodies and could be introduced into a lower vertebrate, a vertebrate other than a primate.
• the antibodies may be used in a variety of ways in histology, cytology, immunoassays, in vivo and in vitro diagnosis, therapy, and the like.
• the antibodies will be conjugated, covalently or non-covalently, to a wide variety of materials, such as labels, particularly labels providing a signal, particles, and cells.
• Labels include radionuclides, dyes, fluorescers, chemiluminescers, enzymes, substrates, cofactors, naturally occurring receptors and ligands, and the like.
• Particles may include magnetic particles, fluorescent particles, porous latex particles, and the like.
• Cells include sheep red blood cells, S. aureus cells, or other cell strains having a particular property or function.
• Freshly drawn human peripheral blood in ACD anticoagulant (adenine-citrate-dextrose) is diluted 1:1 with sterile isotonic saline at room temperature.
• the diluted blood (25ml) is overlayed on a cushion of 10ml of Lymphocyte Separation Medium (LSM, Litton Bionetics) in sterile tubes.
• LSM Lymphocyte Separation Medium
• the tubes are centrifuged at 400xg for 25min at room temperature.
• the lymphocyte/monocyte fraction of cells is collected from the interface plus one-half the volume of LSM.
• the collected cells are diluted 3-fold in serum-free RPMI 1640 and pelleted at 200xg for 10min at room temperature.
• the resulting cell pellets are washed 3x in serum-free RPMI 1640 and the washed cells are counted via hemacytometer and trypan blue vital dye.
• AET-SRBC aminoethylisothiouronium bromide - sheep red blood cells
• a mixture of 2ml containing 1.25x 7 washed PBL, 0.25ml AET-SRBC (10% suspension) 50:1 ratio, and 2.25ml RPMI 1640 - 15% fetal calf serum (FCS) is prepared and centrifuged at 200xg for 5min at 4°C. After incubating undisturbed for 2hrs at 4°C, the pellet is gently resuspended, underlayed with approximately 2ml LSM per tube at 4°C and centrifuged at 400xg for 20min at 4°C.
• E-PBL T-cell depleted PBL
• the human lymphoblastoid cell line GM 1500 (Human Genetic Mutant Cell Repository, Camden, New Jersey) is cultured for 24hrs in medium containing 300pg/ml of ethyl methansulfonate (Sigma Co.). Following the mutagensis with ethyl methansulfonate, the surviving cells are subcultured into increasing concentrations of the purine analog, 6-thioguanine (6TG). After several months, a vigourously growing mutant cell line is established which dies in HAT supplemented medium and is designated as 1A2.
• the cloned cell line 1A2 has been deposited at the ATCC on March 26, 1982 with accession no. CRL-8119.
• the 1A2 cells are harvested from log phased cultures and washed once in serum-free RPMI 1640.
• the E PBL and 1A2 cells are mixed in a 2:1 ratio and pelleted at 160xg for 5min at room temperature.
• the cell pellet is resuspended in RPMI 1640 - 15% FCS, 1mM sodium pyruvate, 2mM L-glutamine and HAT (H-1 ⁇ 10 -4 M; A-1 ⁇ 10 -5 M, T-4 ⁇ 10 -5 M) at 37°C.
• the final subconcentrations are 4x10 cells/ml for E PBL and 2 ⁇ 10 5 cells/ml for 1A2.
• the clonal lines were found to contain the normal diploid number, 46 chromosomes.
• the cells had human surface immunoglobulin as detected by immunofluorescence, using a fluorescein-conjugated F(ab') 2 anti-human Ig.
• the cells were also found to contain Epstein-Barr nuclear antigen (EBNA) as does the 1A2 cell line.
• EBNA Epstein-Barr nuclear antigen
• a radioimmunoassay specific for the human gamma chain was used to measure the IgG content of supernatant fluids from 48 hour log phase cultures and four day higher density cultures of clonal B-lines. Between 50-350ng/ml IgG were produced at 48hrs, while higher density cultures of the same cells produced up to 8pg/ml. Over four months of culture and reassay, the cloned transformants did not demonstrate any change in the quantity or class of secreted immunoglobulins.
• the subject cell-driven process When compared to the properties of supernatant- initiated EBV transformation of human B-cells, the subject cell-driven process has a number of demonstrated advantages.
• the rate of emergence of the transformants is faster. With 12 independent experiments using the lA2 cell line and 12 different normal PBL donors, in each instance, the newly generated transformants grew to 75% confluency in 10-14 days. In addition, the observed efficiency of cell-driven transformation is substantially higher. From SDS-PAGE analysis and subsequent cloning studies, it was calcul.ated that an average of 200 transformed lines were generated per 8x10 E-PBL, i.e. up to 1 B cell line per 40,000 E-PBL. Since monocytes were not depleted, the efficiency in these experiments may be an increment greater.
• the subject method provides a number of advantages over prior art methods.
• stable immortalized cells are obtained.
• the resulting immortalized Ig producing cells do not regress or slough off genes encoding the immunoglobulin of interest.
• the subject cells provide long term stable production of the desired immunoglobulin.
• the subject method is much more efficient in the number of recipient cells which are transformed. It is therefore feasible to use the subject method as a screen of a patient's B-lymphocyte repertoire, particularly where the immune system has been primed due to the presence of a tumor or pathogen or due to an autoimmune disease. Also, as compared to earlier results with EBV transformation, a high percentage of the immortalized Ig producing cells produce. IgG, rather than IgM. Since IgM generally has a lower affinity for its homologous ligand than IgG, for many purposes IgM is not useful.
• the subject method is simple, reproducible, safe and efficient and can be used with any cell capable of producing Ig from a host for EBV.

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• 1982
  • 1982-04-05 US US06/365,218 patent/US4464465A/en not_active Expired - Lifetime
  • 1982-11-25 CA CA000416400A patent/CA1187010A/en not_active Expired
  • 1982-12-14 DE DE8282306667T patent/DE3276706D1/de not_active Expired
  • 1982-12-14 EP EP82306667A patent/EP0090898B1/de not_active Expired
• 1983
  • 1983-03-29 JP JP58051753A patent/JPS58201723A/ja active Granted
• 1987
  • 1987-10-28 JP JP62270483A patent/JPS63126484A/ja active Granted

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